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5-iodo-1-(morpholin-4-ylmethyl)-1H-indole-2,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64258-86-2

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64258-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64258-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,5 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64258-86:
(7*6)+(6*4)+(5*2)+(4*5)+(3*8)+(2*8)+(1*6)=142
142 % 10 = 2
So 64258-86-2 is a valid CAS Registry Number.

64258-86-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodo-1-(morpholin-4-ylmethyl)indole-2,3-dione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64258-86-2 SDS

64258-86-2Downstream Products

64258-86-2Relevant academic research and scientific papers

Effects of isatin N-mannich bases of HeLa cells

Maysinger,Ban,Movrin

, p. 932 - 935 (2007/10/02)

A congeneric series of 5-haloisatins was synthesised and tested for biological activity. Mannich bases and hydrazones of 5-chloro- and 5-iodoisatin were prepared and their structures were determined spectrophotometrically. Morphological deformations and inhibition of radiolabelled precursor incorporation into DNA were studied in HeLa cell culture; antimitotic activity was examined using a phyto test with Lepidium sativum L. I50 values were determined for the most interesting compounds. The results obtained can be interpreted in terms of the group contributions to the parent molecule. Introduction of iodine into the aromatic moiety of isatin (position 5) considerably increased inhibitory potency of the parent molecule. Furthermore, N-bis-(2-chloroethyl) and N-bis-(2-hydroxyethyl) groups, respectively, as amino components of some of the N-Mannich bases, markedly enhance the biological activities studied in this work.

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